Heterogeneous catalysts for hydroamination reactions:: structure-activity relationship

被引:78
|
作者
Penzien, JC
Haessner, C
Jentys, A
Köhler, K
Müller, TE
Lercher, JA
机构
[1] Tech Univ Munich, Lehrstuhl Tech Chem 2, D-85747 Garching, Germany
[2] Tech Univ Munich, Inst Anorgan Chem, D-85747 Garching, Germany
关键词
hydroamination; addition; amines; zeolite BEA; ion exchange; copper; zinc; X-ray absorption; EPR; catalysis;
D O I
10.1016/S0021-9517(03)00283-5
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The catalytic activity of ion-exchanged zeolite BEA for hydroamination reactions, such as the cyclization of 6-aminohex-1-yne and 3-aminopropylvinyl ether and the intermolecular addition of aniline to phenylacetylene, was studied. The most active catalysts were Cu(I)/HBEA, Rh(I)/H-BEA, and Zn/H-BEA. These catalysts were fully characterized and the oxidation state and the local environment of copper, in particular, were explored with XANES and EPR spectroscopy. For Zn/H-BEA zeolites the catalytic activity of the material was related to the local structure around the zinc cations. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:302 / 312
页数:11
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